Target Name: SALL4P7
NCBI ID: G390483
Review Report on SALL4P7 Target / Biomarker Content of Review Report on SALL4P7 Target / Biomarker
SALL4P7
Other Name(s): Spalt-like transcription factor 4 pseudogene 7 | spalt like transcription factor 4 pseudogene 7

SALL4P7: A Potential Drug Target and Biomarker

Introduction

SALL4P7 is a non-coding RNA molecule that has been identified as a Spalt-like transcription factor 4 (SLTF4) gene pseudogene 7. SLTFs are a family of transcription factors that play a crucial role in the regulation of gene expression. They are characterized by the presence of a specific domain, known as the SLTF4 motif, which is responsible for their unique transcription activity. SALL4P7 is one of the SLTF4 gene pseudogenes that has been identified and is currently under investigation as a potential drug target or biomarker.

Expression and Functions of SALL4P7

SALL4P7 is a highly conserved non-coding RNA molecule that is expressed in a variety of tissues and cells. It is primarily expressed in the brain, heart, and testes, and has been shown to play a role in the regulation of gene expression in these tissues. SALL4P7 is a key player in the regulation of stem cell proliferation and has been shown to be involved in the development and maintenance of various tissues, including the brain.

One of the most significant functions of SALL4P7 is its role in the regulation of stem cell proliferation. Stem cells are a type of cell that have the ability to self-renew and differentiate into any cell type in the body. is critical for the development and maintenance of tissues and organs, and SALL4P7 plays a crucial role in this process.

SALL4P7 has also been shown to play a role in the regulation of cell adhesion. Cells adhesion is the process by which cells stick together to form tissues and organs. SALL4P7 is involved in the regulation of cell adhesion by promoting the interaction between cells and by the formation of tight junctions, which are a type of cell-cell adhesion.

In addition to its role in stem cell proliferation and cell adhesion, SALL4P7 has also been shown to play a role in the regulation of gene expression. SALL4P7 has been shown to interact with a variety of transcription factors, including Myb, Prm1, and Prm2. These transcription factors are responsible for regulating the expression of genes that are essential for the maintenance of tissue and organ function.

Drug Targeting and Biomarkers

The potential drug targeting of SALL4P7 is based on its role in the regulation of stem cell proliferation and cell adhesion. Drugs that are able to inhibit the activity of SALL4P7 or its downstream targets can potentially be used to treat a variety of diseases, including cancer, neurodegenerative diseases, and developmental disorders.

One of the most promising compounds that has been shown to inhibit the activity of SALL4P7 is 纬-secretase inhibitor (纬-si) 152. 纬-si152 is a small molecule that is able to inhibit the activity of SALL4P7 and its downstream targets. Studies have shown that 纬-si152 is able to significantly reduce the migration and invasion of cancer cells, indicating that it has the potential to be a useful cancer therapeutic.

In addition to its potential use as a cancer therapeutic, SALL4P7 and its downstream targets may also be useful biomarkers for the diagnosis and monitoring of various diseases. For example, SALL4P7 has been shown to be involved in the regulation of stem cell proliferation and has been linked to the development and maintenance of various tissues, including the brain. Therefore, SALL4P7 and its downstream targets may be useful biomarkers for the diagnosis and monitoring of diseases such as neurodegenerative disorders, cancer, and developmental disorders

Protein Name: Spalt Like Transcription Factor 4 Pseudogene 7

The "SALL4P7 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about SALL4P7 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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SALRNA2 | SAMD1 | SAMD10 | SAMD11 | SAMD12 | SAMD12-AS1 | SAMD13 | SAMD14 | SAMD15 | SAMD3 | SAMD4A | SAMD4A-AS1 | SAMD4B | SAMD5 | SAMD7 | SAMD8 | SAMD9 | SAMD9L | SAMHD1 | SAMM50 | SAMMSON | SAMSN1 | SAMSN1-AS1 | SANBR | SAP130 | SAP18 | SAP30 | SAP30-DT | SAP30BP | SAP30L | SAP30L-AS1 | SAPCD1 | SAPCD1-AS1 | SAPCD2 | SAR1A | SAR1B | SARAF | SARDH | SARM1 | SARNP | SARS1 | SARS2 | SART1 | SART3 | SASH1 | SASH3 | SASS6 | SAT1 | SAT1-DT | SAT2 | SATB1 | SATB1-AS1 | SATB2 | SATB2-AS1 | SATL1 | SAV1 | SAXO1 | SAXO2 | SAYSD1 | SBDS | SBDSP1 | SBF1 | SBF1P1 | SBF2 | SBF2-AS1 | SBK1 | SBK2 | SBK3 | SBNO1 | SBNO2 | SBSN | SBSPON | SC5D | SCAANT1 | SCAF1 | SCAF11 | SCAF4 | SCAF8 | SCAI | SCAMP1 | SCAMP1-AS1 | SCAMP2 | SCAMP3 | SCAMP4 | SCAMP5 | SCAND1 | SCAND2P | SCAND3 | SCAP | SCAPER | SCARA3 | SCARA5 | SCARB1 | SCARB2 | SCARF1 | SCARF2 | SCARNA1 | SCARNA10 | SCARNA11 | SCARNA12